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Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
January 16, 2008
Non-infectious causes of elevated procalcitonin and C-reactive protein serum levels in pediatric patients with hematologic and oncologic disorders
Hans Jürgen Dornbusch, Volker Strenger, Petra Sovinz, et al.
Human Mutation
|
January 1, 1995
Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome)
E Popowska, M Rathmann, A Tylki-Szymanska, et al.
Neurology
|
September 15, 2005
Oculogyric dystonic states in early-onset parkinsonism with basal ganglia calcifications
B Kis, K Hedrich, M Kann, et al.
Journal of Cardiovascular Pharmacology
|
October 1, 1989
Reduced effects of dopexamine on force of contraction in the failing human heart despite preserved beta 2-adrenoceptor subpopulation
M Böhm, B Pieske, P Schnabel, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
June 13, 1998
Unchanged protein expression of sarcoplasmic reticulum Ca2+-ATPase, phospholamban, and calsequestrin in terminally failing human myocardium
G Münch, B Bölck, S Hoischen, et al.
European Journal of Haematology
|
July 22, 2006
Long-term use of anagrelide in the treatment of children with essential thrombocythemia
Herwig Lackner, Christian Urban, Martin Benesch, et al.
Pediatric Transplantation
|
April 14, 2007
Durable remission following a third allogeneic stem cell transplantation in a patient with repeatedly relapsing SAA. The importance of stroma cells for sustained engraftment?
Daniela Weber-Mzell, Christian Urban, Martin Benesch, et al.
Medical Physics
|
May 1, 1988
Modifying constrained least-squares restoration for application to single photon emission computed tomography projection images
B C Penney, M A King, R B Schwinger, et al.
Human Heredity
|
January 1, 1989
X-chromosomal DNA polymorphisms in two ethnic groups from India
P K Seth, C Meissner, W Kress, et al.
Human Molecular Genetics
|
August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)
S Bunge, C Steglich, M Beck, et al.
Page
of 85
Search research articles
Search
Showing results (481-490 of 849) with videos related to
Sort By:
Page
of 85
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
January 16, 2008
Non-infectious causes of elevated procalcitonin and C-reactive protein serum levels in pediatric patients with hematologic and oncologic disorders
Hans Jürgen Dornbusch, Volker Strenger, Petra Sovinz, et al.
Human Mutation
|
January 1, 1995
Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome)
E Popowska, M Rathmann, A Tylki-Szymanska, et al.
Neurology
|
September 15, 2005
Oculogyric dystonic states in early-onset parkinsonism with basal ganglia calcifications
B Kis, K Hedrich, M Kann, et al.
Journal of Cardiovascular Pharmacology
|
October 1, 1989
Reduced effects of dopexamine on force of contraction in the failing human heart despite preserved beta 2-adrenoceptor subpopulation
M Böhm, B Pieske, P Schnabel, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
June 13, 1998
Unchanged protein expression of sarcoplasmic reticulum Ca2+-ATPase, phospholamban, and calsequestrin in terminally failing human myocardium
G Münch, B Bölck, S Hoischen, et al.
European Journal of Haematology
|
July 22, 2006
Long-term use of anagrelide in the treatment of children with essential thrombocythemia
Herwig Lackner, Christian Urban, Martin Benesch, et al.
Pediatric Transplantation
|
April 14, 2007
Durable remission following a third allogeneic stem cell transplantation in a patient with repeatedly relapsing SAA. The importance of stroma cells for sustained engraftment?
Daniela Weber-Mzell, Christian Urban, Martin Benesch, et al.
Medical Physics
|
May 1, 1988
Modifying constrained least-squares restoration for application to single photon emission computed tomography projection images
B C Penney, M A King, R B Schwinger, et al.
Human Heredity
|
January 1, 1989
X-chromosomal DNA polymorphisms in two ethnic groups from India
P K Seth, C Meissner, W Kress, et al.
Human Molecular Genetics
|
August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)
S Bunge, C Steglich, M Beck, et al.
Page
of 85